Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-0156-2016 — Smith & Nephew MOSAICPLASTY DP- Disposable Harvesting System 4.5 mm, Sterile Part Number: 7209235 Intended Use: For arthroscopic (knee and ankle) and open osteochondral grafting fix for osteochondral (cartilage) defects.

U.S. FDA — Device Enforcement · United States · 2015-09-10 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-0156-2016
Date of alert: 2015-09-10
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Smith & Nephew, Inc., Endoscopy Div.
Product category: device
Product type: Devices
Barcode (EAN/GTIN): 50051865

Reported risk: Sterility of device is compromised due to breach in the packaging

Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.

Recall Z-0156-2016 — Smith & Nephew MOSAICPLASTY DP- Disposable Harvesting System 4.5 mm, Sterile Part Number: 7209235 Intended Use: For arthroscopic (knee and ankle) and open osteochondral grafting fix for osteochondral (cartilage) defects.

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